HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epinephrine → (2S)-3-(4-hydroxyphenyl)-2-nitramidopropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epinephrine | HCID 5816 | — |
| Reactant | Arachidonic Acid | HCID 444899 | — |
| Reactant | Prostaglandin H2 | HCID 445049 | — |
| Reactant | HCID 178511350 | HCID 178511350 | — |
| Catalyst | Ferriheme hydroxide | HCID 27337 | — |
| Solvent | Phosphate | HCID 1061 | — |
| Product | (2S)-3-(4-hydroxyphenyl)-2-nitramidopropanoic acid | HCID 9834478 | — |
Reaction Steps
Reaction mixture in 100 mM phosphate buffer, pH 7.4, (total volume, 200 μl) was incubated at 37° C. for 30 minutes. The reaction mixture contained a combination of cytochrome c (40 μg), ovine prostaglandin H2 synthase form 2 (104 units), arachidonic acid (590 μM), epinephrine (31 μg), hematin (1 μM), and DETA NONOate, an NO donor, (300 μM) as indicated in FIG. 2. After incubation, the proteins were separated by SDS-PAGE followed by Western blot analysis with an alkaline phosphatase system using monoclonal antibodies produced against nitrotyrosine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06812212B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-76199e79b92a4202aea748587ed7142b |
| Source note | uspto-grants-2004_11 |